Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_assertion description "[A significant association with CM was found for the long allele of monoamine oxidase A 30 bp VNTR and CYP1A2*1F variant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_assertion evidence source_evidence_literature NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_assertion SIO_000772 20213484 NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_assertion wasDerivedFrom befree-20140225 NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_assertion wasGeneratedBy ECO_0000203 NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP842675.RAPMHO235hFajf-WI98tBXhVX76B0FcSydnIrO6glgePw130_provenance.